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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Authors :
van der Lee, Sven J
Conway, Olivia J
Jansen, Iris
Carrasquillo, Minerva M
Kleineidam, Luca
van den Akker, Erik
Hernández, Isabel
van Eijk, Kristel R
Stringa, Najada
Chen, Jason A
Zettergren, Anna
Andlauer, Till F M
Diez-Fairen, Monica
Simon-Sanchez, Javier
Lleó, Alberto
Zetterberg, Henrik
Nygaard, Marianne
Blauwendraat, Cornelis
Savage, Jeanne E
Mengel-From, Jonas
Moreno-Grau, Sonia
Wagner, Michael
Fortea, Juan
Keogh, Michael J
Blennow, Kaj
Skoog, Ingmar
Friese, Manuel A
Pletnikova, Olga
Zulaica, Miren
Lage, Carmen
de Rojas, Itziar
Riedel-Heller, Steffi
Illán-Gala, Ignacio
Wei, Wei
Jeune, Bernard
Orellana, Adelina
Then Bergh, Florian
Wang, Xue
Hulsman, Marc
Beker, Nina
Tesi, Niccolo
Morris, Christopher M
Indakoetxea, Begoña
Collij, Lyduine E
Scherer, Martin
Morenas-Rodríguez, Estrella
Ifgc
Raffaele, Ferrari
Hernandez, Dena G.
Nalls, Michael A.
Rohrer, Jonathan D.
Adaikalavanramasamy
Kwok, John B. J.
Carol, Dobson-Stone
Brooks, William S.
Schofield, Peterr.
Halliday, Glenda M.
Hodges, John R.
Olivier, Piguet
Laurenbartley
Elizabeth, Thompson
Eric, Haan
Isabel, Hernández
Agustín, Ruiz
Mercè, Boada
Barbara, Borroni
Alessandro, Padovani
Carlos, Cruchaga
Cairns, Nigel J.
Luisa, Benussi
Giuliano, Binetti
Roberta, Ghidoni
Gianluigiforloni
Daniela, Galimberti
Chiara, Fenoglio
Maria, Serpente
Elio, Scarpini
Jordi, Clarimón
Alberto, Lleó
Rafael, Blesa
Maria Landqvist Waldö
Karinnilsson
Christer, Nilsson
Mackenzie, Ian R. A.
Hsiung, Ging-Yuek R.
Mann, DavidM. A.
Jordan, Grafman
Morris, Christopher M.
Johannes, Attems
Griffiths, Timothy D.
Mckeith, Ian G.
Thomas, Alan J.
Pietrini, P.
Huey, Edward D.
Wassermann, Eric M.
Atik, Baborie
Evelyn, Jaros
Tierney, Michael C.
Pau, Pastor
Cristina, Razquin
Sara, Ortega-Cubero
Elena, Alonso
Robertperneczky
Janine, Diehl-Schmid
Panagiotis, Alexopoulos
Alexander, Kurz
Rainero, Innocenzo
Rubino, Elisa
Pinessi, Lorenzo
Ekaterina, Rogaeva
George-Hyslop, Peterst.
Giacomina, Rossi
Fabrizio, Tagliavini
Giorgio, Giaccone
Rowe, James B.
Schlachetzki, Johannes C. M.
James, Uphill
John, Collinge
Simon, Mead
Adrian, Danek
Van Deerlin, Vivianna M.
Murray, Grossman
Trojanowski, John Q.
Julie van der Zee
William, Deschamps
Tim, Vanlangenhove
Marc, Cruts
Christine Van Broeckhoven
Cappa, Stefano F.
Isabelle Le Ber
Didier, Hannequin
Véronique, Golfier
Martine, Vercelletto
Alexis, Brice
Benedetta, Nacmias
Sandro, Sorbi
Silvia, Bagnoli
Irene, Piaceri
Nielsen, Jørgen E.
Hjermind, Lena E.
Matthias, Riemenschneider
Manuelmayhaus
Bernd, Ibach
Gilles, Gasparoni
Sabrina, Pichler
Wei, Gu
Rossor, Martin N.
Fox, Nick C.
Warren, Jason D.
Maria Grazia Spillantini
Morris, Huw R.
Patrizia, Rizzu
Peter, Heutink
Snowden, Julie S.
Sara, Rollinson
Annarichardson
Alexander, Gerhard
Bruni, Amalia C.
Raffaele, Maletta
Fran-cesca, Frangipane
Chiara, Cupidi
Livia, Bernardi
Maria, Anfossi
Maura, Gallo
Maria Elena Conidi
Nicoletta, Smirne
Rosa, Rademakers
Matt, Baker
Dickson, Dennis W.
Graff-Radford, Neill R.
Petersen, Ronald C.
Davidknopman
Josephs, Keith A.
Boeve, Bradley F.
Parisi, Joseph E.
Seeley, William W.
Miller, Bruce L.
Karydas, Anna M.
Howard, Rosen
Vanswieten, John C.
Dopper, Elise G. P.
Harro, Seelaar
Pijnenburg, Yolande A. L.
Philipscheltens
Giancarlo, Logroscino
Rosa, Capozzo
Valeria, Novelli
Puca, Annibale A.
Massimo, Franceschi
Alfredo, Postiglione
Graziella, Milan
Paolosorrentino
Mark, Kristiansen
Huei-Hsin, Chiang
Caroline, Graff
Florencepasquier
Adeline, Rollin
Vincent, Deramecourt
Florence, Lebert
Dimitrioskapogiannis
Luigi, Ferrucci
Stuart, Pickering-Brown
Singleton, Andrew B.
John, Hardy
Parastoo, Momeni
Ironside, James W
van Berckel, Bart N M
Alcolea, Daniel
Wiendl, Heinz
Strickland, Samantha L
Pastor, Pau
Rodríguez Rodríguez, Eloy
Boeve, Bradley F
Petersen, Ronald C
Ferman, Tanis J
van Gerpen, Jay A
Reinders, Marcel J T
Uitti, Ryan J
Tárraga, Lluís
Maier, Wolfgang
Dols-Icardo, Oriol
Kawalia, Amit
Dalmasso, Maria Carolina
Boada, Mercè
Zettl, Uwe K
van Schoor, Natasja M
Beekman, Marian
Allen, Mariet
Masliah, Eliezer
de Munain, Adolfo López
Pantelyat, Alexander
Wszolek, Zbigniew K
Ross, Owen A
Dickson, Dennis W
Graff-Radford, Neill R
Knopman, David
Rademakers, Rosa
Lemstra, Afina W
Pijnenburg, Yolande A L
Scheltens, Philip
Gasser, Thomas
Chinnery, Patrick F
Hemmer, Bernhard
Huisman, Martijn A
Troncoso, Juan
Moreno, Fermin
Nohr, Ellen A
Sørensen, Thorkild I A
Heutink, Peter
Sánchez-Juan, Pascual
Posthuma, Danielle
Clarimón, Jordi
Christensen, Kaare
Ertekin-Taner, Nilüfer
Scholz, Sonja W
Ramirez, Alfredo
Ruiz, Agustín
Slagboom, Eline
van der Flier, Wiesje M
Holstege, Henne
Complex Trait Genetics
Amsterdam Neuroscience - Complex Trait Genetics
Sociology
The Social Context of Aging (SoCA)
Universidad de Cantabria
DESGESCO Dementia Genetics
EADB Alzheimer Dis European
IFGC Int FTD-Genomics
IPDGC Int Parkinson Dis Genomics
RiMod-FTD Risk Modifying
Netherlands Brain Bank NBB
GIFT Genetic Invest
van der Lee, Sven J [0000-0003-1606-8643]
Andlauer, Till FM [0000-0002-2917-5889]
Tesi, Niccolo [0000-0002-1413-5091]
Scheltens, Philip [0000-0002-1046-6408]
Holstege, Henne [0000-0002-7688-3087]
Apollo - University of Cambridge Repository
Amsterdam Neuroscience - Neurodegeneration
Neurology
Epidemiology and Data Science
Radiology and nuclear medicine
Other Research
Divisions
APH - Societal Participation & Health
APH - Aging & Later Life
Human genetics
Amsterdam Reproduction & Development (AR&D)
APH - Personalized Medicine
APH - Methodology
Source :
ACTA NEUROPATHOLOGICA, r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, instname, van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernandez, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleo, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illan-Gala, I, Wei, W, Jeune, B, Orellana, A, Bergh, F T, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodriguez, E, Ironside, J W, van Berckel, B N M, Alcolea, D, Wiendl, H, Strickland, S L, Pastor, P, Rodriguez Rodriguez, E, Boeve, B F, Petersen, R C, Ferman, T J, van Gerpen, J A, Reinders, M J T, Uitti, R J, Tarraga, L, Maier, W, Dols-Icardo, O, Kawalia, A, Dalmasso, M C, Boada, M, Zettl, U K, van Schoor, N M, Beekman, M, Allen, M, Masliah, E, Lopez de Munain, A, Pantelyat, A, Wszolek, Z K, Ross, O A, Dickson, D W, Graff-Radford, N R, Knopman, D, Rademakers, R, Lemstra, A W, Pijnenburg, Y A L, Scheltens, P, Gasser, T, Chinnery, P F, Hemmer, B, Huisman, M A, Troncoso, J, Moreno, F, Nohr, E A, Sørensen, T I A, Heutink, P, Sanchez-Juan, P, Posthuma, D, Clarimon, J, Christensen, K, Ertekin-Taner, N, Scholz, S W, Ramirez, A, Ruiz, A, Slagboom, E, van der Flier, W M & Holstege, H 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8, Acta neuropathologica 138(2), 237-250 (2019). doi:10.1007/s00401-019-02026-8, Dipòsit Digital de Documents de la UAB, Universitat Autònoma de Barcelona, Acta Neuropathologica, 138(2), CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET, Acta Neuropathologica, Acta Neuropathologica, 138(2), 237-250. Springer Verlag, Acta Neuropathol . 2019 Aug;138(2):237-250., Acta neuropathologica, UCrea Repositorio Abierto de la Universidad de Cantabria, Universidad de Cantabria (UC), 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB) & The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8, van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Hulsman, M, Beker, N, Tesi, N, Collij, L E, van Berckel, B N M, Reinders, M J T, van Schoor, N M, Lemstra, A W, Pijnenburg, Y A L, Scheltens, P, Huisman, M A, Heutink, P, Posthuma, D, van der Flier, W M, Holstege, H, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB) & The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8, Acta Neuropathologica, 138(2), 237-250
Publication Year :
2019

Abstract

ATENCIÓ: la correcció està també al DDD, cal relacionar??? https://ddd.uab.cat/record/226203 Altres ajuts: The following studies and consortia have contributed to this manuscript. Amsterdam dementia Cohort (ADC): Research of the Alzheimer center Amsterdam is part of the neurodegeneration research program of Amsterdam Neuroscience. The Alzheimer Center Amsterdam is supported by Stichting Alzheimer Nederland and Stichting VUmc fonds. The clinical database structure was developed with funding from Stichting Dioraphte. Genotyping of the Dutch case-control samples was performed in the context of EADB (European Alzheimer DNA biobank) funded by the JPco-fuND FP-829-029 (ZonMW projectnumber 733051061). 100-Plus study: We are grateful for the collaborative efforts of all participating centenarians and their family members and/or relations. This work was supported by Stichting Alzheimer Nederland (WE09.2014-03), Stichting Diorapthe, horstingstuit foundation, Memorabel (ZonMW projectnumber 733050814) and Stichting VUmc Fonds. Genotyping of the 100-Plus Study was performed in the context of EADB (European Alzheimer DNA biobank) funded by the JPco-fuND FP-829-029 (ZonMW projectnumber 733051061). German Study on Ageing, Cognition and Dementia in Primary Care Patients (AgeCoDe): This study/publication is part of the German Research Network on Dementia (KND), the German Research Network on Degenerative Dementia (KNDD; German Study on Ageing, Cognition and Dementia in Primary Care Patients; AgeCoDe), and the Health Service Research Initiative (Study on Needs, health service use, costs and health-related quality of life in a large sample of oldest-old primary care patients (85+; AgeQualiDe)) and was funded by the German Federal Ministry of Education and Research (grants KND: 01GI0102, 01GI0420, 01GI0422, 01GI0423, 01GI0429, 01GI0431, 01GI0433, 01GI0434; grants KNDD: 01GI0710, 01GI0711, 01GI0712, 01GI0713, 01GI0714, 01GI0715, 01GI0716; grants Health Service Research Initiative: 01GY1322A, 01GY1322B, 01GY1322C, 01GY1322D, 01GY1322E, 01GY1322F, 01GY1322G). Alfredo Ramirez was partly supported by the ADAPTED consortium: Alzheimer's disease Apolipoprotein Pathology for Treatment Elucidation and Development, which has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No 115975. Brain compendium: This work was funded by the UK Medical Research Council (13044). P.F.C. is a Wellcome Trust principal Fellow (212219/Z/18/Z) and a UK NIHR Senior Investigator, who receives support from the Medical Research Council Mitochondrial Biology Unit (MC_UU_00015/9), and the National Institute for Health Research (NIHR) Biomedical Research Centre based at Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR, or the Department of Health.Clinical AD, Sweden: We would like to thank UCL Genomics for performing the genotyping analyses. Danish data: The studies behind the Danish long-lived cases received funding from The National Program for Research Infrastructure 2007 (grant no. 09-063256), the Danish Agency for Science Technology and Innovation, the Velux Foundation, the US National Institute of Health (P01 AG08761), the Danish Agency for Science, Technology and Innovation/The Danish Council for Independent Research (grant no. 11-107308), the European Union's Seventh Framework Programme (FP7/2007-2011) under grant agreement no. 259679, the INTERREG 4 A programme Syddanmark-Schleswig-K.E.R.N. (by EU funds from the European Regional Development Fund), the CERA Foundation (Lyon), the AXA Research Fund, Paris, and The Health Foundation (Helsefonden), Copenhagen, Denmark. The GOYA study was conducted as part of the activities of the Danish Obesity Research Centre (DanORC, www.danorc.dk) and The MRC centre for Causal Analyses in Translational Epidemiology (MRC CAiTE). The genotyping for GOYA was funded by the Wellcome Trust (WT 084762). GOYA is a nested study within The Danish National Birth Cohort which was established with major funding from the Danish National Research Foundation. Additional support for this cohort has been obtained from the Pharmacy Foundation, the Egmont Foundation, The March of Dimes Birth Defects Foundation, the Augustinus Foundation, and the Health Foundation. Fundació ACE (FACE): We would like to thank patients and controls who participated in this project. We are indebted to Trinitat Port-Carbó and her family for their support of Fundació ACE research programs. Fundació ACE collaborates with the Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED, Spain) and is one of the participating centers of the Dementia Genetics Spanish Consortium (DEGESCO). Agustín Ruiz has received support from the EU/EFPIA Innovative Medicines Initiative Joint Undertaking ADAPTED Grant No. 115975 and by grants PI13/02434 and PI16/01861. Acción Estratégica en Salud, integrated in the Spanish National R + D + I Plan and financed by ISCIII (Instituto de Salud Carlos III)-Subdirección General de Evaluación and the Fondo Europeo de Desarrollo Regional (FEDER- "Una manera de Hacer Europa"), by Fundación bancaria "La Caixa" and Grifols SA (GR@ACE project). Genetics of Healthy Ageing Study (GEHA - NL): The work described in this paper was funded mainly by the EU GEHA Project contract no. LSHM-CT-2004-503-270. Gothenburg Birth Cohort (GBC) Studies: We would like to thank UCL Genomics for performing the genotyping analyses. The studies were supported by The Stena Foundation, The Swedish Research Council (2015-02830, 2013-8717), The Swedish Research Council for Health, Working Life and Wellfare (2013-1202, 2005-0762, 2008-1210, 2013-2300, 2013-2496, 2013-0475), The Brain Foundation, Sahlgrenska University Hospital (ALF), The Alzheimer's Association (IIRG-03-6168), The Alzheimer's Association Zenith Award (ZEN-01-3151), Eivind och Elsa K:son Sylvans Stiftelse, The Swedish Alzheimer Foundation. International FTD-Genomics Consortium (IFGC): International FTD-Genomics Consortium (IFGC): The authors thank the IFGC for providing relevant data to support the analyses presented in this manuscript. Further acknowledgments for IFGC (https://ifgcsite.wordpress.com/), e.g. full members list and affiliations, are found in the online supplementary files. IPDGC (​The International Parkinson Disease Genomics Consortium): We also would like to thank all members of the International Parkinson Disease Genomics Consortium (IPDGC). See for a complete overview of members, acknowledgements and funding http://pdgenetics.org/partners. Kompetenznetz Multiple Sklerose (KKNMS): This work was supported by the German Ministry for Education and Research (BMBF) as part of the "German Competence Network Multiple Sclerosis" (KKNMS) (grant nos. 01GI0916 and 01GI0917) and the Munich Cluster for Systems Neurology (SyNergy). TA was supported by the BMBF through the Integrated Network IntegraMent, under the auspices of the e:Med Programme (01ZX1614J). BH was supported by the EU Horizon 2020 project MultipleMS.Longitudinal Aging Study Amsterdam (LASA) is largely supported by a grant from the Netherlands Ministry of Health, Welfare and Sports, Directorate of Long-Term Care. The authors are grateful to all LASA participants, the fieldwork team and all researchers for their ongoing commitment to the study. Leiden Longevity Study: This study was supported by a grant from the Innovation-Oriented Research Program on Genomics (SenterNovem IGE05007), the Centre for Medical Systems Biology, and the Netherlands Consortium for Healthy Ageing (Grant 050-060-810), all in the framework of the Netherlands Genomics Initiative/Netherlands Organization for Scientific Research (NWO) and by Unilever Colworth.Maria Carolina Dalmasso: Georg Forster Research Award (Alexander von Humboldt Foundation). Mayo Clinic AD, DLB, PD, PSP: We thank the patients and their families for their participation, without whom these studies would not have been possible. Funding for this work was supported by National Institute on Aging [RF AG051504 to NET.; U01 AG046139 to NET]; and National Institute of Neurological Disorders and Stroke [R01 NS080820 to NET; P50 NS072187]. The Mayo Clinic is a Lewy Body Dementia Association (LBDA) Research Center of Excellence, American Parkinson Disease Association (APDA) Information and Referral Center and Center for Advanced Research, NINDS Tau Center without Walls (U54-NS100693) and is supported by Mayo Clinic AD and related dementias genetics program, The Little Family Foundation, the Mangurian Foundation for Lewy body research and NINDS R01 NS078086 (to OAR). The PD program at the Mayo Clinic Florida is also supported by the Mayo Clinic Center for Regenerative Medicine, Mayo Clinic Center for Individualized Medicine, Mayo Clinic Neuroscience Focused Research Team (Cecilia and Dan Carmichael Family Foundation, and the James C. and Sarah K. Kennedy Fund for Neurodegenerative Disease Research at Mayo Clinic in Florida), the gift from Carl Edward Bolch, Jr., and Susan Bass Bolch, and The Sol Goldman Charitable Trust. Samples included in this study are from the brain bank at Mayo Clinic in Jacksonville which is supported by CurePSP The online version of this article (10.1007/s00401-019-02026-8) contains supplementary material, which is available to authorized users.

Details

Language :
English
ISSN :
00016322
Volume :
138
Issue :
2
Database :
OpenAIRE
Journal :
Acta Neuropathologica
Accession number :
edsair.doi.dedup.....236c815c1d8287553434b852a305ebcb
Full Text :
https://doi.org/10.1007/s00401-019-02026-8